Canonical Allele Identifier: CA1148224851
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197101675T= , CM000663.2:g.197101675T= GRCh38
NC_000001.10:g.197070805T= , CM000663.1:g.197070805T= GRCh37
NC_000001.9:g.195337428T= NCBI36
NG_015867.1:g.50020A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367408.6:n.2108-5511A=
ENST00000367409.9:c.7576A= MANE Select ENSP00000356379.4:p.Asn2526=
ENST00000680265.1:c.7576A= ENSP00000505384.1:p.Asn2526=
ENST00000680710.1:c.7576A= ENSP00000506676.1:p.Asn2526=
ENST00000294732.11:c.4066-5511A= ENSP00000294732.7:n.4066-5511A=
ENST00000367408.5:c.1816-5511A= ENSP00000356378.1:n.1816-5511A=
ENST00000367409.8:c.7576A= ENSP00000356379.4:p.Asn2526=
ENST00000612785.1:c.1534A= ENSP00000479244.1:p.Asn512=
NM_001206846.1:c.4066-5511A= NP_001193775.1:n.4066-5511A=
NM_018136.4:c.7576A= NP_060606.3:p.Asn2526=
NM_018136.5:c.7576A= MANE Select NP_060606.3:p.Asn2526=
NM_001206846.2:c.4066-5511A= NP_001193775.1:n.4066-5511A=